John D. Overton
Active 2008–2025
- 96
- Papers
- 20,256
- Citations
- 56
- h-index
- 94
- i10-index
Citations
Citation sources
Countries
Institutions
- Harvard University1.3%
- Broad Institute1%
- Massachusetts General Hospital0.9%
- Yale University0.7%
- University of Pennsylvania0.7%
- Inserm0.6%
- Other94.8%
Fields
- Medicine45.5%
- Biochemistry, Genetics and Molecular Biology41.4%
- Neuroscience6.3%
- Immunology and Microbiology3.6%
- Psychology0.8%
- Computer Science0.5%
- Other1.9%
Topics
- Genetic Associations and Epidemiology6.1%
- Genomics and Rare Diseases4%
- Genetics and Neurodevelopmental Disorders2.9%
- Liver Disease Diagnosis and Treatment2.7%
- Autism Spectrum Disorder Research2.2%
- Diabetes, Cardiovascular Risks, and Lipoproteins2%
- Other80.1%
Coauthors
- Aris Baras42
- Jeffrey G. Reid34
- Luca A. Lotta19
- Alan R. Shuldiner18
- Xiaodong Bai18
- Michael Cantor16
- Alexander Lopez14
- Claudia Gonzaga‐Jauregui14
- Evan K. Maxwell14
- Giovanni Coppola14
- Gonçalo R. Abecasis14
- Marcus B. Jones14
- Suganthi Balasubramanian14
- Colm O’Dushlaine13
- Joshua Backman13
- Lukas Habegger13
- Aris N. Economides12
- Cristopher V. Van Hout12
- Frederick E. Dewey12
- Joelle Mbatchou12
- Joseph B. Leader12
- Anthony Marcketta11
- Jack A. Kosmicki11
- Jeffrey Staples11
All papers
- Exome sequencing and analysis of 454,787 UK Biobank participants
Authors: Joshua Backman, Alexander Li, Anthony Marcketta, Dylan Sun, Joelle Mbatchou, Michael D. Kessler, Christian Benner, Daren Liu, Adam E. Locke, Suganthi Balasubramanian, Ashish Yadav, Nilanjana Banerjee, Christopher E. Gillies, Amy Damask, Simon Liu, Xiaodong Bai, Alicia Hawes, Evan K. Maxwell, Lauren Gurski, Kyoko Watanabe, Jack A. Kosmicki, Veera M. Rajagopal, Jason Mighty, DiscovEHR, Marcus B. Jones, Lyndon J. Mitnaul, Eli A. Stahl, Giovanni Coppola, Eric Jorgenson, Lukas Habegger, William Salerno, Alan R. Shuldiner, Luca A. Lotta, John D. Overton, Michael Cantor, Jeffrey G. Reid, George D. Yancopoulos, Hyun Min Kang, Jonathan Marchini, Aris Baras, Gonçalo R. Abecasis, Manuel A. R. Ferreira - Nature 2021 cited by 1,077
- Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ancestry meta-analysis
Authors: Marijana Vujković, Jacob M. Keaton, Julie A. Lynch, Donald R. Miller, Jin Zhou, Catherine Tcheandjieu, Jennifer E. Huffman, Themistocles L. Assimes, Kimberly Lorenz, Xiang Zhu, Austin T. Hilliard, Renae Judy, Jie Huang, Kyung Min Lee, Derek Klarin, Saiju Pyarajan, John Danesh, Olle Melander, Asif Rasheed, Nadeem Hayat Mallick, Shahid Hameed, Irshad Hussain Qureshi, Muhammad Afzal, Uzma Malik, Anjum Jalal, Shahid Abbas, Xin Sheng, Long Gao, Klaus H. Kaestner, Katalin Suszták, Yan V. Sun, Scott L. DuVall, Kelly Cho, Jennifer S. Lee, J. Michael Gaziano, Lawrence S. Phillips, James B. Meigs, Peter D. Reaven, Peter W.F. Wilson, Todd L. Edwards, Daniel J. Rader, Scott M. Damrauer, Christopher J. O’Donnell, Philip S. Tsao, Mark A. Atkinson, Al C. Powers, Ali Naji, Klaus H. Kaestner, Gonçalo R. Abecasis, Aris Baras, Michael Cantor, Giovanni Coppola, Aris N. Economides, Luca A. Lotta, John D. Overton, Jeffrey G. Reid, Alan R. Shuldiner, Christina Beechert, Caitlin Forsythe, Erin D. Fuller, Zhenhua Gu, Michael Lattari, Alexander Lopez, Thomas D. Schleicher, Maria Sotiropoulos Padilla, Karina Toledo, Louis Widom, Sarah E. Wolf, Manasi Pradhan, Kia Manoochehri, Ricardo H. Ulloa, Xiaodong Bai, Suganthi Balasubramanian, Leland Barnard, Andrew Blumenfeld, Gisu Eom, Lukas Habegger, Alicia Hawes, Shareef Khalid, Evan K. Maxwell, William Salerno, Jeffrey Staples, Ashish Yadav, Marcus B. Jones, Lyndon J. Mitnaul, VA Million Veteran Program, Samuel M. Aguayo, Sunil K. Ahuja, Zuhair K. Ballas, Sujata Bhushan, Edward J. Boyko, David Cohen, John Concato, Joseph I. Constans, Louis J. Dell’Italia, Joseph Fayad, Ronald Fernando, Hermes Flórez, Melinda A. Gaddy, Saib Gappy and 82 more - Nature Genetics 2020 cited by 801
- A Protein-Truncating HSD17B13 Variant and Protection from Chronic Liver Disease
Authors: Noura S. Abul‐Husn, Xiping Cheng, Alexander Li, Yurong Xin, Claudia Schurmann, Panayiotis E. Stevis, Yashu Liu, Julia Kozlitina, Stefan Stender, G. Craig Wood, Ann Stepanchick, Matthew Still, Shane McCarthy, Colm O’Dushlaine, Jonathan S. Packer, Suganthi Balasubramanian, Nehal Gosalia, David Esopi, Sun Y. Kim, Semanti Mukherjee, Alexander Lopez, Erin D. Fuller, John S. Penn, Xin Chu, Jonathan Z. Luo, Uyenlinh L. Mirshahi, David J. Carey, Christopher D. Still, Michael D. Feldman, Aeron Small, Scott M. Damrauer, Daniel J. Rader, Brian Zambrowicz, William C. Olson, Andrew Murphy, Ingrid B. Borecki, Alan R. Shuldiner, Jeffrey G. Reid, John D. Overton, George D. Yancopoulos, Helen H. Hobbs, Jonathan C. Cohen, Omri Gottesman, Tanya M. Teslovich, Aris Baras, Tooraj Mirshahi, Jesper Gromada, Frederick E. Dewey - New England Journal of Medicine 2018 cited by 805
- Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations
Authors: Cindy G. Boer, Konstantinos Hatzikotoulas, Lorraine Southam, Lilja Stefánsdóttir, Yanfei Zhang, Rodrigo Coutinho de Almeida, Tian Wu, Jie Zheng, April Hartley, Maris Teder‐Laving, Anne Heidi Skogholt, Chikashi Terao, Eleni Zengini, George Alexiadis, Andrei Barysenka, Gyða Björnsdóttir, Maiken E. Gabrielsen, Arthur Gilly, Þorvaldur Ingvarsson, Marianne Bakke Johnsen, Helgi Jónsson, M. Kloppenburg, Almut Luetge, Sigrún H. Lund, Reedik Mägi, Massimo Mangino, Rob G. H. H. Nelissen, Manu Shivakumar, Julia Steinberg, Hiroshi Takuwa, Laurent F. Thomas, Margo Tuerlings, John Loughlin, Nigel Arden, Fraser Birrell, Andrew Carr, Panos Deloukas, Michael Doherty, Andrew W. McCaskie, William Ollier, Ashok Rai, Stuart H. Ralston, Tim D. Spector, Gillian A. Wallis, Amy E. Martinsen, Cristen J. Willer, Egil A. Fors, Ingunn Mundal, Knut Hagen, Kristian Bernhard Nilsen, Marie Udnesseter Lie, Sigrid Børte, Ben Brumpton, Jonas B. Nielsen, Lars G. Fritsche, Wei Zhou, Ingrid Heuch, Kjersti Storheim, Evangelos Tyrpenou, A. Koukakis, Dimitrios Chytas, Dimitrios Stergios Evangelopoulos, Chronopoulos Efstathios, Spiros G. Pneumaticos, Vasileios S. Nikolaou, Κonstantinos Ν. Malizos, Lydia Anastasopoulou, Gonçalo R. Abecasis, Aris Baras, Michael Cantor, Giovanni Coppola, Andrew Deubler, Aris N. Economides, Luca A. Lotta, John D. Overton, Jeffrey G. Reid, Alan R. Shuldiner, Katia Karalis, Katherine Siminovitch, Christina Beechert, Caitlin Forsythe, Erin D. Fuller, Zhenhua Gu, Michael Lattari, Alexander Lopez, Thomas D. Schleicher, Maria Sotiropoulos Padilla, Louis Widom, Sarah E. Wolf, Manasi Pradhan, Kia Manoochehri, Xiaodong Bai, Suganthi Balasubramanian, Boris Boutkov, Gisu Eom, Lukas Habegger, Alicia Hawes, Olga Krasheninina, Rouel Lanche, Adam J. Mansfield and 55 more - Cell 2021 cited by 467
- Common and rare variant associations with clonal haematopoiesis phenotypes
Authors: Michael D. Kessler, Amy Damask, Sean O’Keeffe, Nilanjana Banerjee, Dadong Li, Kyoko Watanabe, Anthony Marketta, Michael Van Meter, Stefan Semrau, Julie Horowitz, Jing Tang, Jack A. Kosmicki, Veera M. Rajagopal, Yuxin Zou, Yariv Houvras, Arkopravo Ghosh, Christopher E. Gillies, Joelle Mbatchou, Ryan R. White, Niek Verweij, Jonas Bovijn, Neelroop Parikshak, Michelle G. LeBlanc, Marcus B. Jones, David J. Glass, Luca A. Lotta, Michael Cantor, Gurinder S. Atwal, Adam E. Locke, Manuel A. R. Ferreira, Raquel P. Deering, Charles Paulding, Alan R. Shuldiner, Gavin Thurston, Adolfo A. Ferrando, Will Salerno, Jeffrey G. Reid, John D. Overton, Jonathan Marchini, Hyun Min Kang, Aris Baras, Gonçalo R. Abecasis, Eric Jorgenson - Nature 2022 cited by 304
- Genetic and Pharmacologic Inactivation of ANGPTL3 and Cardiovascular Disease
Authors: Frederick E. Dewey, Viktoria Gusarova, Richard L. Dunbar, Colm O’Dushlaine, Claudia Schurmann, Omri Gottesman, Shane McCarthy, Cristopher V. Van Hout, Shannon Bruse, Hayes M. Dansky, Joseph B. Leader, Michael F. Murray, Marylyn D. Ritchie, H. Lester Kirchner, Lukas Habegger, Alex Lopez, John S. Penn, An Sha Zhao, Weiping Shao, Neil Stahl, Andrew Murphy, Sara Hamon, Aurelie Bouzelmat, Rick Zhang, Brad Shumel, Robert Pordy, Daniel A. Gipe, Gary Herman, Wayne Huey‐Herng Sheu, I‐Te Lee, Kae‐Woei Liang, Xiuqing Guo, Jerome I. Rotter, Yii‐Der I. Chen, William E. Kraus, Svati H. Shah, Scott M. Damrauer, Aeron Small, Daniel J. Rader, Anders Berg Wulff, Børge G. Nordestgaard, Anne Tybjærg‐Hansen, Anita M. van den Hoek, Hans M.G. Princen, David H. Ledbetter, David J. Carey, John D. Overton, Jeffrey G. Reid, William J. Sasiela, Poulabi Banerjee, Alan R. Shuldiner, Ingrid B. Borecki, Tanya M. Teslovich, George D. Yancopoulos, Scott Mellis, Jesper Gromada, Aris Baras - New England Journal of Medicine 2017 cited by 875
- Exome sequencing and characterization of 49,960 individuals in the UK Biobank
Authors: Cristopher V. Van Hout, Ioanna Tachmazidou, Joshua Backman, Joshua Hoffman, Daren Liu, Ashutosh Kumar Pandey, Claudia Gonzaga‐Jauregui, Shareef Khalid, Bin Ye, Nilanjana Banerjee, Alexander Li, Colm O’Dushlaine, Anthony Marcketta, Jeffrey Staples, Claudia Schurmann, Alicia Hawes, Evan K. Maxwell, Leland Barnard, Alexander Lopez, John S. Penn, Lukas Habegger, Andrew Blumenfeld, Xiaodong Bai, Sean O’Keeffe, Ashish Yadav, Kavita Praveen, Marcus B. Jones, William Salerno, Wendy K. Chung, Ida Surakka, Cristen J. Willer, Kristian Hveem, Joseph B. Leader, David J. Carey, David H. Ledbetter, Lon R. Cardon, George D. Yancopoulos, Aris N. Economides, Giovanni Coppola, Alan R. Shuldiner, Suganthi Balasubramanian, Michael Cantor, Matthew R. Nelson, John C. Whittaker, Jeffrey G. Reid, Jonathan Marchini, John D. Overton, Robert A. Scott, Gonçalo R. Abecasis, Laura M. Yerges-Armstrong, Aris Baras - Nature 2020 cited by 636
- Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects
Authors: Laurence J. Howe, Michel G. Nivard, Tim Morris, Ailin Falkmo Hansen, Humaira Rasheed, Yoonsu Cho, Geetha Chittoor, Rafael Ahlskog, Penelope A. Lind, Teemu Palviainen, Matthijs D. van der Zee, Rosa Cheesman, Massimo Mangino, Yunzhang Wang, Shuai Li, Lucija Klaric, Scott M. Ratliff, Lawrence F. Bielak, Marianne Nygaard, Alexandros Giannelis, Emily A. Willoughby, Chandra A. Reynolds, Jared V. Balbona, Ole A. Andreassen, Helga Ask, Aris Baras, Christopher R. Bauer, Dorret I. Boomsma, Archie Campbell, Harry Campbell, Zhengming Chen, Paraskevi Christofidou, Elizabeth C. Corfield, Christina C. Dahm, Deepika Dokuru, Luke M. Evans, Eco J. C. de Geus, Sudheer Giddaluru, Scott D. Gordon, K. Paige Harden, W. David Hill, Amanda Hughes, Shona M. Kerr, Yongkang Kim, Hyeokmoon Kweon, Antti Latvala, Debbie A. Lawlor, Liming Li, Kuang Lin, Per Magnus, Patrik K. E. Magnusson, Travis T. Mallard, Pekka Martikainen, Melinda C. Mills, Pål R. Njølstad, John D. Overton, Nancy L. Pedersen, David J. Porteous, Jeffrey G. Reid, Karri Silventoinen, Melissa C. Southey, Camilla Stoltenberg, Elliot M. Tucker–Drob, Margaret J. Wright, Hyeokmoon Kweon, Philipp Koellinger, Daniel J. Benjamin, Patrick Turley, Laurence J. Howe, Michel G. Nivard, Tim Morris, Ailin Falkmo Hansen, Humaira Rasheed, Yoonsu Cho, Geetha Chittoor, Rafael Ahlskog, Penelope A. Lind, Teemu Palviainen, Matthijs D. van der Zee, Rosa Cheesman, Massimo Mangino, Yunzhang Wang, Shuai Li, Lucija Klaric, Scott M. Ratliff, Lawrence F. Bielak, Marianne Nygaard, Alexandros Giannelis, Emily A. Willoughby, Chandra A. Reynolds, Jared V. Balbona, Ole A. Andreassen, Helga Ask, Dorret I. Boomsma, Archie Campbell, Harry Campbell, Zhengming Chen, Paraskevi Christofidou, Elizabeth C. Corfield, Christina C. Dahm and 96 more - Nature Genetics 2022 cited by 393
- De novo mutations revealed by whole-exome sequencing are strongly associated with autism
Authors: Stephan Sanders, Michael T. Murtha, Abha R. Gupta, John D. Murdoch, Melanie J. Raubeson, A. Jeremy Willsey, A. Gulhan Ercan‐Sencicek, Nicholas M. DiLullo, Neelroop Parikshak, Jason L. Stein, Michael F. Walker, G Ober, Nicole A. Teran, Youeun Song, Paul El-Fishawy, Ryan Murtha, Murim Choi, John D. Overton, Robert Bjornson, Nicholas Carriero, Kyle A. Meyer, Kaya Bilgüvar, Shrikant Mane, Nenad Šestan, Richard P. Lifton, Murat Günel, Kathryn Roeder, Daniel H. Geschwind, Bernie Devlin, Matthew W. State - Nature 2012 cited by 2,183
- Sequencing of 640,000 exomes identifies GPR75 variants associated with protection from obesity
Authors: Parsa Akbari, Ankit Gilani, Olukayode Sosina, Jack A. Kosmicki, Lori Khrimian, Yi‐Ya Fang, Trikaldarshi Persaud, Víctor Garcia, Dylan Sun, Alexander Li, Joelle Mbatchou, Adam E. Locke, Christian Benner, Niek Verweij, Nan Lin, Sakib Hossain, Kevin Agostinucci, Jonathan V. Pascale, Ercument Dirice, Michael E. Dunn, William E. Kraus, Svati H. Shah, Yii‐Der I. Chen, Jerome I. Rotter, Daniel J. Rader, Olle Melander, Christopher D. Still, Tooraj Mirshahi, David J. Carey, Jaime Berúmen, Pablo Kuri‐Morales, Jesús Alegre-Díaz, Jason Torres, Jonathan Emberson, Rory Collins, Suganthi Balasubramanian, Alicia Hawes, Marcus Herbert Jones, Brian Zambrowicz, Andrew Murphy, Charles Paulding, Giovanni Coppola, John D. Overton, Jeffrey G. Reid, Alan R. Shuldiner, Michael Cantor, Hyun Min Kang, Gonçalo R. Abecasis, Katia Karalis, Aris N. Economides, Jonathan Marchini, George D. Yancopoulos, Mark W. Sleeman, Judith Y. Altarejos, Giusy Della Gatta, Roberto Tapia-Conyer, Michal L. Schwartzman, Aris Baras, Manuel A. R. Ferreira, Luca A. Lotta - Science 2021 cited by 276
- Advancing human genetics research and drug discovery through exome sequencing of the UK Biobank
Authors: Joseph D. Szustakowski, Suganthi Balasubramanian, Erika Kvikstad, Shareef Khalid, Paola G. Bronson, Ariella Sasson, Emily Wong, Daren Liu, J. Wade Davis, Carolina Haefliger, A. Katrina Loomis, Rajesh Mikkilineni, Hyun Ji Noh, Samir Wadhawan, Xiaodong Bai, Alicia Hawes, Olga Krasheninina, Ricardo H. Ulloa, Alex E. Lopez, Erin N. Smith, Jeffrey F. Waring, Christopher D. Whelan, Ellen Tsai, John D. Overton, William Salerno, Howard J. Jacob, Sándor Szalma, Heiko Runz, Gregory Hinkle, Paul Nioi, Slavé Petrovski, Melissa Miller, Aris Baras, Lyndon J. Mitnaul, Jeffrey G. Reid, Oleg Moiseyenko, Carlos Garcia Rios, Saurabh Saha, Gonçalo R. Abecasis, Nilanjana Banerjee, Christina Beechert, Boris Boutkov, Michael Cantor, Giovanni Coppola, Aris N. Economides, Gisu Eom, Caitlin Forsythe, Erin D. Fuller, Zhenhua Gu, Lukas Habegger, Marcus B. Jones, Rouel Lanche, Michael Lattari, Michelle G. LeBlanc, Dadong Li, Luca A. Lotta, Kia Manoochehri, Adam J. Mansfield, Evan K. Maxwell, Jason Mighty, Mrunali Nafde, Sean O’Keeffe, Max Orelus, Maria Sotiropoulos Padilla, Razvan Panea, Tommy Polanco, Manasi Pradhan, Ayesha Rasool, Thomas D. Schleicher, Deepika Sharma, Alan R. Shuldiner, Jeffrey Staples, Cristopher V. Van Hout, Louis Widom, Sarah E. Wolf, Sally John, Chia‐Yen Chen, David Sexton, Varant Kupelian, Eric Marshall, T. Swan, Susan Eaton, Jimmy Z. Liu, Stephanie Loomis, Megan E. Jensen, Saranya Duraisamy, Jason Tetrault, David Merberg, Sunita Badola, Mark Reppell, Jason Grundstad, Xiuwen Zheng, Aimée M. Deaton, Margaret M. Parker, Lucas D. Ward, Alexander O. Flynn-Carroll, Caroline A. Austin, Ruth March, Menelas N. Pangalos, Adam Platt and 11 more - Nature Genetics 2021 cited by 427
- De novo mutations in histone-modifying genes in congenital heart disease
Authors: Samir Zaidi, Murim Choi, Hiroko Wakimoto, Lijiang Ma, Jianming Jiang, John D. Overton, Angela Romano-Adesman, Robert Bjornson, Roger E. Breitbart, Kerry K. Brown, Nicholas Carriero, Yee Him Cheung, John Deanfield, Steven R. DePalma, Khalid A. Fakhro, Joseph Glessner, Håkon Håkonarson, Michael J. Italia, Jonathan R. Kaltman, Juan Pablo Kaski, Richard Kim, Jennie Kline, Teresa Lee, Jeremy Leipzig, Alexander Lopez, Shrikant Mane, Laura E. Mitchell, Jane W. Newburger, Michael Parfenov, Itsik Pe’er, George A. Porter, Amy E. Roberts, Ravi Sachidanandam, Stephan Sanders, Howard Seiden, Mathew W. State, Sai Lakshmi Subramanian, Irina R. Tikhonova, Wei Wang, Dorothy Warburton, Peter S. White, Ismée A. Williams, Hongyu Zhao, Jonathan G. Seidman, Martina Brueckner, Wendy K. Chung, Bruce D. Gelb, Elizabeth Goldmuntz, Christine E. Seidman, Richard P. Lifton - Nature 2013 cited by 968
- Genome-wide association study of alcohol consumption and use disorder in 274,424 individuals from multiple populations
Authors: Henry R. Kranzler, Hang Zhou, Rachel L. Kember, Rachel Vickers‐Smith, Amy C. Justice, Scott M. Damrauer, Philip S. Tsao, Derek Klarin, Aris Baras, Jeffrey G. Reid, John D. Overton, Daniel J. Rader, Zhongshan Cheng, Janet P. Tate, William C. Becker, John Concato, Ke Xu, Renato Polimanti, Hongyu Zhao, Joel Gelernter - Nature Communications 2019 cited by 535
- Analysis of rare genetic variation underlying cardiometabolic diseases and traits among 200,000 individuals in the UK Biobank
Authors: Sean J. Jurgens, Seung Hoan Choi, Valerie N. Morrill, Mark Chaffin, James P. Pirruccello, Jennifer L. Halford, Lu‐Chen Weng, Victor Nauffal, Carolina Roselli, Amelia Weber Hall, Matthew T. Oetjens, Braxton Lagerman, David P. vanMaanen, Gonçalo R. Abecasis, Xiaodong Bai, Suganthi Balasubramanian, Aris Baras, Christina Beechert, Boris Boutkov, Michael Cantor, Giovanni Coppola, Tanima De, Andrew Deubler, Aris N. Economides, Gisu Eom, Manuel A. R. Ferreira, Caitlin Forsythe, Erin D. Fuller, Zhenhua Gu, Lukas Habegger, Alicia Hawes, Marcus B. Jones, Katia Karalis, Shareef Khalid, Olga Krasheninina, Rouel Lanche, Michael Lattari, Dadong Li, Alexander Lopez, Luca A. Lotta, Kia Manoochehri, Adam J. Mansfield, Evan K. Maxwell, Jason Mighty, Lyndon J. Mitnaul, Mona Nafde, Jonas B. Nielsen, Sean O’Keeffe, Max Orelus, John D. Overton, Maria Sotiropoulos Padilla, Razvan Panea, Tommy Polanco, Manasi Pradhan, Ayesha Rasool, Jeffrey G. Reid, William Salerno, Thomas D. Schleicher, Alan R. Shuldiner, Katherine Siminovitch, Jeffrey Staples, Ricardo H. Ulloa, Niek Verweij, Louis Widom, Sarah E. Wolf, Krishna G. Aragam, Kathryn L. Lunetta, Christopher M. Haggerty, Steven A. Lubitz, Patrick T. Ellinor - Nature Genetics 2022 cited by 173
- Inactivating Variants in ANGPTL4 and Risk of Coronary Artery Disease
Authors: Frederick E. Dewey, Viktoria Gusarova, Colm O’Dushlaine, Omri Gottesman, Jesus Trejos, Charleen Hunt, Cristopher V. Van Hout, Lukas Habegger, David G. Buckler, Ka-Man V. Lai, Joseph B. Leader, Michael F. Murray, Marylyn D. Ritchie, H. Lester Kirchner, David H. Ledbetter, John S. Penn, Alexander Lopez, Ingrid B. Borecki, John D. Overton, Jeffrey G. Reid, David J. Carey, Andrew Murphy, George D. Yancopoulos, Aris Baras, Jesper Gromada, Alan R. Shuldiner - New England Journal of Medicine 2016 cited by 510
- Germline Mutations in CIDEB and Protection against Liver Disease
Authors: Niek Verweij, Mary E. Haas, Jonas B. Nielsen, Olukayode Sosina, Minhee Kim, Parsa Akbari, Tanima De, George Hindy, Jonas Bovijn, Trikaldarshi Persaud, Lawrence Miloscio, Mary Germino, Lampros Panagis, Kyoko Watanabe, Joelle Mbatchou, Marcus B. Jones, Michelle G. LeBlanc, Suganthi Balasubramanian, Craig Lammert, Sofia Enhörning, Olle Melander, David J. Carey, Christopher D. Still, Tooraj Mirshahi, Daniel J. Rader, Prodromos Parasoglou, Johnathon R. Walls, John D. Overton, Jeffrey G. Reid, Aris N. Economides, Michael Cantor, Brian Zambrowicz, Andrew Murphy, Gonçalo R. Abecasis, Manuel A. R. Ferreira, Ēriks Šmagris, Viktoria Gusarova, Mark W. Sleeman, George D. Yancopoulos, Jonathan Marchini, Hyun Min Kang, Katia Karalis, Alan R. Shuldiner, Giusy Della Gatta, Adam E. Locke, Aris Baras, Luca A. Lotta - New England Journal of Medicine 2022 cited by 121
- Genomic Analysis of Non- NF2 Meningiomas Reveals Mutations in TRAF7 , KLF4 , AKT1 , and SMO
Authors: Victoria Clark, E. Zeynep Erson‐Omay, Akdes Serin, Jun Yin, Justin Cotney, Koray Özduman, Timuçin Avşar, Jie Li, Phillip B. Murray, Octavian Henegariu, Saliha Yılmaz, Jennifer Moliterno Günel, Geneive Carrión-Grant, Baran Yılmaz, Conor Grady, Bahattin Tanrıkulu, Mehmet Bakırcıoğlu, Hande Kaymakçalan, Ahmet Okay Çağlayan, Leman Sencar, Emre Ceyhun, Ahmet Atik, Yaşar Bayri, Hanwen Bai, Luis Kolb, Ryan Hebert, Sacit Bulent Omay, Ketu Mishra-Gorur, Murim Choi, John D. Overton, Eric C. Holland, Shrikant Mane, Matthew W. State, Kaya Bilgüvar, Joachim M. Baehring, Philip H. Gutin, Joseph M. Piepmeier, Alexander O. Vortmeyer, Cameron Brennan, M. Necmettin Pamir, Türker Kılıç, Richard P. Lifton, James P. Noonan, Katsuhito Yasuno, Murat Günel - Science 2013 cited by 904
- Mutation of NLRC4 causes a syndrome of enterocolitis and autoinflammation
Authors: Neil Romberg, Khatoun Al Moussawi, Carol Nelson‐Williams, Amy L. Stiegler, Erin Loring, Murim Choi, John D. Overton, Eric Meffre, Mustafa K. Khokha, Anita Hüttner, Brian L. West, Nikolai A. Podoltsev, Titus J. Boggon, Barbara I. Kazmierczak, Richard P. Lifton - Nature Genetics 2014 cited by 510
- Genetic identification of familial hypercholesterolemia within a single U.S. health care system
Authors: Noura S. Abul‐Husn, Kandamurugu Manickam, Laney K. Jones, Eric A. Wright, Dustin N. Hartzel, Claudia Gonzaga‐Jauregui, Colm O’Dushlaine, Joseph B. Leader, H. Lester Kirchner, D’Andra M. Lindbuchler, Marci L Barr, Monica A. Giovanni, Marylyn D. Ritchie, John D. Overton, Jeffrey G. Reid, Raghu Metpally, Amr H. Wardeh, Ingrid B. Borecki, George D. Yancopoulos, Aris Baras, Alan R. Shuldiner, Omri Gottesman, David H. Ledbetter, David J. Carey, Frederick E. Dewey, Michael F. Murray - Science 2016 cited by 428
- Patients With High Genome-Wide Polygenic Risk Scores for Coronary Artery Disease May Receive Greater Clinical Benefit From Alirocumab Treatment in the ODYSSEY OUTCOMES Trial
Authors: Amy Damask, Philippe Gabríel Steg, Gregory G. Schwartz, Michael Szarek, Emil Hagström, Lina Badimón, M. John Chapman, Cathérine Boileau, Sotirios Tsimikas, Henry N. Ginsberg, Poulabi Banerjee, Garen Manvelian, Robert Pordy, Sibylle Hess, John D. Overton, Luca A. Lotta, George D. Yancopoulos, Gonçalo R. Abecasis, Aris Baras, Charles Paulding - Circulation 2019 cited by 246
- Distribution and clinical impact of functional variants in 50,726 whole-exome sequences from the DiscovEHR study
Authors: Frederick E. Dewey, Michael F. Murray, John D. Overton, Lukas Habegger, Joseph B. Leader, Samantha N. Fetterolf, Colm O’Dushlaine, Cristopher V. Van Hout, Jeffrey Staples, Claudia Gonzaga‐Jauregui, Raghu Metpally, Sarah A. Pendergrass, Monica A. Giovanni, H. Lester Kirchner, Suganthi Balasubramanian, Noura S. Abul‐Husn, Dustin N. Hartzel, Daniel R. Lavage, Korey A. Kost, Jonathan S. Packer, Alexander Lopez, John S. Penn, Semanti Mukherjee, Nehal Gosalia, Manoj Kanagaraj, Alexander Li, Lyndon J. Mitnaul, Lance J. Adams, Thomas N. Person, Kavita Praveen, Anthony Marcketta, Matthew S. Lebo, Christina Austin‐Tse, Heather Mason‐Suares, Shannon Bruse, Scott Mellis, Robert S. Phillips, Neil Stahl, Andrew Murphy, Aris N. Economides, Kimberly A. Skelding, Christopher D. Still, James R. Elmore, Ingrid B. Borecki, George D. Yancopoulos, F. Daniel Davis, W. Andrew Faucett, Omri Gottesman, Marylyn D. Ritchie, Alan R. Shuldiner, Jeffrey G. Reid, David H. Ledbetter, Aris Baras, David J. Carey - Science 2016 cited by 607
- Genome-wide association analyses highlight etiological differences underlying newly defined subtypes of diabetes
Authors: Dina Mansour Aly, Om Prakash Dwivedi, Rashmi B. Prasad, Annemari Käräjämäki, Rebecka Hjort, Manonanthini Thangam, Mikael Åkerlund, Anubha Mahajan, Miriam S. Udler, José C. Florez, Mark I. McCarthy, RGC Management and Leadership Team, Gonçalo R. Abecasis, Aris Baras, Michael Cantor, Giovanni Coppola, Aris N. Economides, Luca A. Lotta, John D. Overton, Jeffrey G. Reid, Alan R. Shuldiner, Sequencing and Lab Operations, Christina Beechert, Caitlin Forsythe, Erin D. Fuller, Zhenhua Gu, Michael Lattari, Alexander Lopez, Thomas D. Schleicher, Maria Sotiropoulos Padilla, Louis Widom, Sarah E. Wolf, Manasi Pradhan, Kia Manoochehri, Ricardo H. Ulloa, Genome Informatics, Xiaodong Bai, Suganthi Balasubramanian, Andrew Blumenfeld, Gisu Eom, Lukas Habegger, Alicia Hawes, Shareef Khalid, Evan K. Maxwell, William Salerno, Jeffrey Staples, Marcus B. Jones, Lyndon J. Mitnaul, Julia Brosnan, Olle Melander, Sofia Carlsson, Ola Hansson, Tiinamaija Tuomi, Leif Groop, Emma Ahlqvist - Nature Genetics 2021 cited by 175
- Genotyping, sequencing and analysis of 140,000 adults from Mexico City
Authors: Andrey Ziyatdinov, Jason Torres, Jesús Alegre-Díaz, Joshua Backman, Joelle Mbatchou, Michael Turner, Sheila M. Gaynor, Tyler Joseph, Yuxin Zou, Daren Liu, Rachel Wade, Jeffrey Staples, Razvan Panea, Alex Popov, Xiaodong Bai, Suganthi Balasubramanian, Lukas Habegger, Rouel Lanche, Alex Lopez, Evan K. Maxwell, Marcus B. Jones, Humberto Garcia‐Ortíz, Raúl Ramírez-Reyes, Rogelio Santacruz-Benítez, Abhishek Nag, Katherine R. Smith, Amy Damask, Nan Lin, Charles Paulding, Mark Reppell, Sebastian Zöllner, Eric Jorgenson, William Salerno, Slavé Petrovski, John D. Overton, Jeffrey G. Reid, Timothy A. Thornton, Gonçalo R. Abecasis, Jaime Berúmen, Lorena Orozco, Rory Collins, RGC Management and Leadership Team, Gonçalo R. Abecasis, Adolfo A. Ferrando, Michael Cantor, Giovanni Coppola, Andrew Deubler, Aris N. Economides, Katia Karalis, Luca A. Lotta, Lyndon J. Mitnaul, John D. Overton, Jeffrey G. Reid, Alan R. Shuldiner, Katherine Siminovitch, Sequencing and Lab Operations, Christina Beechert, Erin D. Brian, Laura M. Cremona, Hang Du, Caitlin Forsythe, Zhenhua Gu, Kristy Guevara, Michael Lattari, Alexander Lopez, Kia Manoochehri, Manasi Pradhan, Raymond Reynoso, Ricardo Schiavo, Maria Sotiropoulos Padilla, Chenggu Wang, Sarah E. Wolf, Amelia Averitt, Nilanjana Banerjee, Dadong Li, Sameer Malhotra, Justin Mower, Mudasar Sarwar, Deepika Sharma, Jeffrey Staples, Jay Sundaram, Sean Yu, Aaron Zhang, Genome Informatics and Data Engineering, Mona Nafde, George Mitra, Sujit Gokhale, Andrew Bunyea, Janice Clauer, Krishna Pawan Punuru, Sanjay Sreeram, Gisu Eom, Benjamin Sultan, Vrushali Mahajan, Eliot Austin, Koteswararao Makkena, Sean O’Keeffe, Tommy Polanco, Ayesha Rasool, William Salerno and 483 more - Nature 2023 cited by 96
- Association of the V122I Hereditary Transthyretin Amyloidosis Genetic Variant With Heart Failure Among Individuals of African or Hispanic/Latino Ancestry
Authors: Scott M. Damrauer, Kumardeep Chaudhary, Judy H. Cho, Lusha W. Liang, Edgar Argulian, Lili Chan, Amanda Dobbyn, Marie Guerraty, Renae Judy, Jenna Kay, Rachel L. Kember, Michael G. Levin, Aparna Saha, Tielman Van Vleck, Shefali S. Verma, JoEllen Weaver, Noura S. Abul‐Husn, Aris Baras, Julio A. Chirinos, Brian Drachman, Eimear E. Kenny, Ruth J. F. Loos, Jagat Narula, John D. Overton, Jeffrey G. Reid, Marylyn D. Ritchie, Giorgio Sirugo, Girish N. Nadkarni, Daniel J. Rader, Ron Do - JAMA 2019 cited by 158
